The Book of Mormon and the Origin of Native Americans from a Maternally Inherited DNA Standpoint
by Ugo A. Perego1
Where do Native Americans come from? When did they arrive in the Western Hemisphere? Which route(s) did they follow? How many colonization events were there? These and other fascinating questions have been at the center of debates among scholars from different disciplines since the rediscovery of the New World by Europeans more than 500 years ago. Archaeologists, linguists, anthropologists, and geneticists are still working on a consensus about the processes that took place through the millennia which resulted in the peopling of America’s double-continent. The considerable number of scholarly papers that have been published on DNA and Amerindians is a demonstration that “despite the 80 year history of genetic studies in the Americas, the real work is now [only] beginning to fully elucidate the genetic history of the two continents.”2
At first, Europeans believed that the New World inhabitants were somewhat connected with the biblical account of the lost ten tribes,3 leading them to look for cultural and linguistic similarities between contemporary Jews and Native Americans.4 The evidence amassed to this point indicates that although sporadic pre-Columbian contacts with the Old World cannot be completely ruled out,5 the majority of Native Americans share a genetic affinity with Asian populations.6
The notion that part or all American Indians are of Hebrew descent is still popular among members of The Church of Jesus Christ of Latter-day Saints (LDS Church or Mormons) as they interpret the Book of Mormon—a volume the LDS Church considers both historical and sacred in nature. In its pages we learn of three relatively small parties (the Jaredites, the Lehites, and the Mulekites) that left their native homeland in the Old World at different times and through divine guidance traveled to a new Promised Land on the American continent. The Book of Mormon contains only marginal information about the demographic dynamics and the internal geography of the land occupied by the people it describes. Instead, the volume claims to be primarily an abridgement of thousands of years of mostly spiritual and religious history and not a full account of the people. For example, the text does not give information about whether other populations were already established in the Americas at the time of the migrants’ arrival. This lack of information leaves many open questions that have profound implications for the genetic characteristics that we would expect to find in present-day Native American populations. The extent to which these Old World groups expanded and colonized their new habitat, the level of admixture they may have experienced with local indigenous populations—if any were present—and the locations of their settlements would all influence the genetic landscape we would observe in Native Americans today. Furthermore, it is implausible that ancient record keepers would have had a comprehensive knowledge of all the goings-on of the entire vast landmass of the Americas, considering that from Northern Canada to Patagonia is about 8,700 miles, a greater distance than that from Portugal to Japan! Despite these many complex factors, since the publication of the Book of Mormon in 1830, Mormons and non-Mormons alike have resorted to speculation in an attempt to fill in the historical and geographical details that are either completely missing or only briefly alluded to in the Book of Mormon text.7
Even in light of statements made by individual LDS Church leaders and Mormon scholars regarding this topic through the years, the LDS Church advocates no official position on the subjects of Book of Mormon geography and the origins of Amerindian populations.8 Together with its members, LDS Church leaders are entitled to their own opinions and reasoning on this subject, as demonstrated by “pre-DNA” comments such as the one given by President Anthony W. Ivins, a member of the First Presidency, at the April 1929 General Conference: “It [the Book of Mormon] does not tell us that no one was here before them [the Book of Mormon peoples]. It does not tell us that people did not come after.”9 Others have expressed similar opinions more recently.10
Over the past decade, critics of the Book of Mormon have promoted the idea that since the majority of Amerindian DNA lineages are closely related to Asian populations, and since no perfect genetic affinity to the Middle East has been found, it must be concluded that the Book of Mormon account is fictional. This argument is sometimes bolstered in part by a common sentiment in the general membership of the Mormon church that all Native Americans are descendants of the Old World migrants described in the Book of Mormon text, and in particular the Israelite group of Lehi and his close associates. To contend with these arguments, some Mormons dismiss DNA studies as being unreliable for reconstructing history, while others are quick to embrace any news of possible Middle Eastern DNA in the Americas as conclusive proof that the migrations to America described in the Book of Mormon are real.
This essay provides an updated review on the properties of mitochondrial DNA (mtDNA) and explains how these pertain to the study of ancient population expansions, specifically focusing on the origin of Native Americans. The majority of background information that supports the following discussion has been presented at length in previous publications,11 and will not be restated herein. The most pertinent supporting material that follows will provide a foundation to the reader regarding the basics of mtDNA heredity, a review and update on the most recent mtDNA data available pertaining to the origins of Native American populations, and a summary of how this information relates to the larger DNA and Book of Mormon discussion. It is important for readers to understand that while mtDNA and other genetic motifs are useful in elucidating some historical questions,12 it may not be possible to achieve a full resolution of questions arising between secular and religious history.
The hereditary features of mtDNA provide unique information that enables the study of the ancient history of humanity based on the foundational principles of population genetics. It is essential to have a working knowledge of these principles when evaluating genetic studies relating to the Book of Mormon, as those presenting arguments against its authenticity overlook some of these concepts.
MtDNA is found in mitochondria (singular mitochondrion), which are the organelles within each cell responsible for life sustaining processes such as cell energy metabolism, cell division, and programmed cell death (apoptosis). Each cell may contain thousands of mitochondria and each mitochondrion may contain hundreds of mtDNA genomes. A significant hereditary feature of mtDNA is that it is maternally inherited, a fact that affects the extent of historical information one can learn from its analysis.
The mtDNA molecule is comprised of only 16,569 bases and is therefore very small when compared to the nuclear genome (the 3.2 billion bases of genetic material that make up the 23 pairs of chromosomes found in the cell’s nucleus). The first complete mtDNA genome was sequenced in 1981 at Cambridge University and it is called the Anderson or Cambridge Reference Sequence (CRS).13 In 1999, Andrews and colleagues re-sequenced the original Cambridge mtDNA, which is now referred to as rCRS.14 This sequence became the industry standard used to compare complete or partial mtDNA data produced to date. Instead of reporting long lists of genetic bases for each mtDNA sample, a typical report only includes differences (i.e., mutations) from the rCRS. This set of mutations is called a haplotype, and it is the mtDNA genetic profile descended from the maternal lineage of an individual. As a general rule, mutational events occur randomly and their accumulation over time has resulted in the differentiation of the many mtDNA lineages observed in today’s world populations. Analysis of these lineages can therefore be structured hierarchically in a tree-like format called a phylogeny (Figure 1). A phylogeny attempts to model the true hereditary history of mtDNA across populations.
Figure 1. Schematic phylogeny of human mtDNA (Alessandro Achilli and Ugo A. Perego, 2009). The four common (A2, B2, C1, and D1) and rarer (D4h3) Native American lineages are nested within the East Asian portion of the tree, while the northern North America X2a is found among the West Eurasian sub-clades (Alessandro Achilli and others, 2008; Ugo A. Perego and others, 2009). Currently, a total of thirteen pre-Columbian mtDNA haplogroups have been identified in the Americas.
Similar to the Y chromosome (Ycs), mtDNA does not recombine with the DNA from the other molecules. That is, mtDNA is inherited as a fully intact DNA segment between generations, with variations from mother to child arising rarely due to random mutations. While the Ycs is inherited along the paternal line, as noted before, mtDNA follows an inheritance pattern found on the opposite side of the family tree, along the unbroken maternal line (Figure 2). A mother’s mtDNA is passed to all of her children, but only the daughters will pass their mtDNA to the next generation. Although there has been one documented instance of male-inherited mtDNA in humans, this is considered an exceptionally rare (almost unique) exception, mainly associated with a pathological status.15
Figure 2. The strict paternal Y chromosome (Ycs) and strict maternal mitochondrial DNA (mtDNA) inheritance patterns.
The mtDNA genome has two parts: the control region,16 which includes three segments called HVS1, HVS2, and HVS3,17 and the coding region (where all the mtDNA’s genes that produce essential proteins to life are found). Acquiring genetic data from an individual’s mtDNA can be ascertained using the following ways, with the amount of information obtained increasing for each successive approach:
- Inspection of Restriction Fragment Length Polymorphisms (RFLPs) using enzymes that break the DNA into smaller fragments at specific short (usually 4-6 base pair) sequences. Depending on the presence or lack of mutations, the fragment will or will not be broken and the resulting fragment length indicates the presence or lack of the mutation;
- Assaying Single Nucleotide Polymorphisms (SNPs), where the type of base at a specific location is identified for comparison with the reference sequence;
- Sequencing of part or all the control region (up to approximately one thousand bases);
- Sequencing of the complete mtDNA genome (all the 16,569 bases—the highest level of mtDNA molecular resolution attainable).
During the 1990s, a large amount of studies were published presenting mtDNA data obtained from RFLP and control region sequences (often only HVS1, ~300 bases), many of them highlighting several Native American populations.18 The mtDNA data produced during that decade allowed scientists to investigate for the first time the mtDNA variation from diverse populations. From this, they advanced the first theories about the origin of anatomically modern humans and the processes of expansion that resulted in the colonization of the continental masses.
Starting around the year 2000, by employing new technological advances, researchers began to produce complete genome sequences as the standard for the most rigorous mtDNA population studies.19 However, the process of generating a full mtDNA sequence is still labor intensive and relatively expensive. Recently, a study reviewing all the published mtDNA full sequences reported that only a very small fraction of these data are of Native American origin (see Figure 3), leaving a considerable gap to fill in the scientific literature.20
Figure 3. Worldwide distribution of all complete mtDNA sequences published in GenBank (http://www.ncbi.nlm.nih.gov/nucleotide) as of August 2008 (Luísa Pereira and others, 2009).
The opportunity to acquire complete mtDNA sequences brought several benefits to the field of population genetics, including:
- Resolving questionable phylogenies based on control region data (this region has a higher mutation rate and is therefore affected by recurring mutations);
- Identification of smaller clades within the large world mtDNA tree;
- Better understanding of events that characterize the expansion and migration routes followed by our early ancestors;
- An improved understanding of the expected mutation rate of the mtDNA genome, yielding a better calibration of the molecular clock—the mathematical underpinnings of historical date estimations based on genetic data.
It is important to remember that population geneticists face the continuing challenge of correlating their findings with those of other disciplines, including linguistics, anthropology, archaeology, and others. A multi-disciplinary approach allows a consensus to be formed for date estimates, and helps to cross-verify findings among different fields of study.21
The differentiation of mtDNA has been generated by the sequential accumulation of new mutations along radiating maternal lineages. Over the course of time, this process of molecular divergence has given rise to separate mtDNA lineages that are now called haplogroups that is, groups of haplotypes sharing similar characteristics. Haplogroups are named following a simple but standardized nomenclature procedure, alternating letters to numbers and starting with a capital letter (e.g., K1a4, H1a, A2d2, C1b2a, etc.) (Figure 1). Coincidentally, the first time haplogroup names were given was when the sequence variation of mtDNAs from Native American populations was investigated. Four major mutational motifs were identified and they were therefore originally named A, B, C, and D, using the first four letters of the alphabet.22
The mtDNA process of molecular differentiation was relatively rapid and occurred mainly during and after the recent process of human colonization and diffusion into different regions and continents. Thus, serendipitously, the different subsets of mtDNA variation tend to be restricted to different geographic areas and population groups. Older mtDNA lineages had more time to accumulate a greater number of mutations, while younger mtDNA lineages accumulated fewer mutations and therefore less variation. Mainstream population geneticists are in agreement that, based on the available mtDNA data, the most recent common female ancestor, from whom all mtDNAs in modern humans derive, lived in Africa about 200,000 years ago and that an initial migration out of Africa took place around 70,000 years ago, represented by a mtDNA lineage known as L3. L3 left the Horn of Africa eastward following a southern coastal route along the Indian Ocean, and while moving further east, about 63,000 years ago, gave rise to two mtDNA “daughter” branches known as haplogroups M and N. An offshoot of N shortly after was haplogroup R. Lineages M, N, and R are the female ancestors of all the known non-African lineages that eventually colonized the rest of the continents. These lineages are also known as macro- or superhaplogroups. The Americas were the last of all the continents to be colonized by Homo sapiens, approximately 10-20,000 years ago (Figure 4).
Figure 4. Multiple dispersals in human evolution. Migrations of humans over time shown through mtDNA data (Alessandro Achilli and Ugo A. Perego, 2007).
The basics of Population Genetics
Using the mtDNA mutations as a guide, it is possible to trace all modern mtDNA lineages back to a single African female ancestor. Geneticists have named this ancestor the African “Eve,” but despite this name, she was not necessarily the only woman on the planet. The mtDNA lineages corresponding to other women simply disappeared either due to chance when their offspring failed to reproduce—a phenomenon known in population genetics as genetic drift—or because of natural or manmade calamities that wiped out a significant portion of the population—an event referred to as a population bottleneck—or because they were selected against due to the detrimental effect of specific mutations. This African “Eve” was the only one that was successful in perpetuating her mtDNA lineage through the generations. Therefore, because of genetic drift, population bottlenecks, or natural selection, the mtDNA lineages observed in today’s population do not reflect the full range of mtDNA variation that occurred throughout human history. A recent example from a study in Iceland based on genetic and genealogical data clearly demonstrated how the majority of people living in that country today are just a small representation of people that lived just 300 years ago.23 This work is a powerful illustration and a rare example of a controlled study where genealogical, historical, and genetic data are available to unequivocally demonstrate the effect of genetic drift and natural selection in a fairly isolated population. The effect of these population genetics processes occur globally (including organisms other than humans) and are not exclusive to the Icelandic population; most relevant to our current discussion, these principles have also affected populations in the Western Hemisphere. Although some would like to dismiss the Icelandic model and suggest that it is more of an exception than the rule,24 these population genetics laws cannot be ignored: they are the fundamental force that shaped the modern genetic landscape worldwide. It is a well known fact that mtDNA lineages have disappeared in the past and that they will continue to disappear in modern times. This process has occurred everywhere in the world and the Americas are no exception.25
Native American DNA
With regards to measuring the genetic variation observed among the indigenous people of the Western Hemisphere, molecular anthropologist Michael H. Crawford has stated this problem succinctly and repeatedly in his volume The Origins of Native Americans:
“The Conquest and its sequelae squeezed the entire Amerindian population through a genetic bottleneck. The reduction of Amerindian gene pools from 1/3 to 1/25 of their previous size implies a considerable loss of genetic variability. […] It is highly unlikely that survivorship was genetically random. […] Thus, the present gene-frequency distributions of Amerindian populations may be distorted by a combination of effects stemming from genetic bottlenecks and natural selection. […] This population reduction has forever altered the genetics of the surviving groups, thus complicating any attempts at reconstructing the pre-Columbian genetic structure of most New World groups.”26
Subsequent research has supported this notion. In an article dealing with ancient DNA from Native American populations that was published in the American Journal of Physical Anthropology, the authors made the following statement: “Genetic drift has been a significant force [on Native American genetics] and, together with a major population crash after the European contact, has altered haplogroup frequencies and caused the loss of many haplotypes.”27
These statements from experts in the field of modern and ancient DNA from Native American populations—who are uninvolved with the Book of Mormon and DNA debate—give insight into the influence of the major population-altering events of the Columbian and pre-Columbian eras on the genetic variation of modern Native Americans. Their mtDNAs were not immune to the evolutionary processes of genetic drift and population bottleneck as they have been observed in a similar fashion in other populations. One cannot overstate the importance of considering both random as well as environmental factors when studying history using DNA samples from modern populations, including that of Amerindians. Population genetics principles guide geneticists who study human history, and genetic drift and population bottlenecks are among the most basic factors to consider in their work.
Some wonder if ancient DNA samples might shed additional light on the history of ancient populations such as the ancestral Native Americans. This approach can be valuable when the necessary samples are available and the DNA is of good quality. Note, however, that several limitations must be carefully considered when studying ancient DNA:
- Accessibility to the ancient remains: in many cases, Native American and First Nation groups consider their burial grounds sacred and are quite resistant to DNA testing being performed on their ancestors. (Moreover, they are often even resistant to testing being done on themselves).28
- Contamination: skeletal remains found in museums or from personal collections may have been handled improperly over time. Thus any attempt to retrieve endogenous DNA from them may be compromised by the presence of DNA belonging to those who have touched the samples since the time of their excavation.
- Confidence that the data obtained is genuine: a general practice when analyzing ancient DNA samples is to compare the data obtained with samples from the modern population. If identical or similar haplotypes are found in the modern population, then it is assumed that the data obtained from the ancient specimen is reliable. However, if no matches are found in the modern population, it can become difficult to ascertain if the data obtained belongs to a lineage no longer in existence or if the genetic signal come from contamination or post-mortem damage.
- Failed sequencing because of environmental factors: even in cases when bone fragments are found and proper excavation techniques are in place, the success rate of extracting and analyzing ancient DNA is approximately 1 in 3. Extreme heat, high humidity, gamma rays from the Sun, etc. can accelerate DNA degradation. During the last decade, thanks to new technological advancements and a better understanding of how to work with ancient DNA,29 results have improved and the data are more reliable. However, much of the data published in the 1990s was susceptible to less rigorous collection and lab procedures that may have resulted in unreliable DNA data and conclusions.
- Limited quantity of data obtained: because ancient DNA is highly degraded, only small fragments of genetic material can be sequenced. Most of the ancient DNA data available in the public literature comes from sequencing short segments of the control region. To date, only a few complete mtDNA sequences (the full 16,569 bases of the mtDNA genome) from ancient human remains have been successfully produced (e.g. five Neanderthals and the Tyrolean Ice Man, Ötzi).30
In summary, even though ancient DNA data has the potential to be extremely helpful in phylogenetic studies and in reconstructing past population events, scientists are still limited by the amount and quality of data they can obtain from ancient remains.
A significant finding that elucidates the usefulness of combining ancient and modern DNA in the study of Native American populations comes from a recent publication featuring a short control region segment sequenced from a ~10,000 year old skeleton found in Alaska.31 Carbon dating confirmed that the remains were clearly pre-Columbian, but the genetic profile obtained did not match any of the earlier identified Amerindian mtDNAs (A2, B2, C1, D1, and X2a). Previously, a number of studies on Native American populations revealed a small quantity of samples labeled as “others,” as they did not belong to any of the known indigenous mtDNA lineages and were thought to have been contaminated or the result of European admixture. Based on the mtDNA data retrieved from the ancient Alaskan specimen, some of those previously unclassified samples were re-examined and are confirmed as belonging to a novel Native American lineage named D4h3.32 Unfortunately, as explained earlier, it is difficult to access and to obtain good quality data from ancient DNA. Therefore, for every reclassified mtDNA lineage, it is probable that many misclassifications remain unknown or unresolved. The case of D4h3 is likely to be a rare event in shedding additional light on the maternal history of Native American populations.
Another serious limitation comes from possibly inappropriate assumptions of what mtDNA candidate haplogroups to expect from the small groups described in the Book of Mormon. A survey of modern populations—including Middle Easterners and Asians—would reveal a certain number of mtDNA lineages that occur at high frequencies and are therefore labeled as region-specific for the modern population, but would also uncover a number of mtDNA haplogroups that are more rare. Most likely, these less frequent mtDNA lineages are the results of relatively recent migratory events, an occurrence very common throughout history because of international trade routes (such as those that took place along the Silk Road) or military expansions (e.g., the Assyrian, Babylonian, Roman, or Mongol empires, just to cite a few). These important historical events are responsible for a partial reshuffling of the DNA compositions of geographic regions throughout the world, adding to the genetic diversity of affected locations. Although the majority of lineages in one region could be considered the typical mtDNA expected to be observed in a specific location in modern populations, the reality is that potentially any given mtDNA lineage could be also found at low frequencies in the same geographic area. Any of these low-frequency haplogroups could be candidates for genetic types that may have been more common during any previous time period within the last few thousand years.
This issue touches on the people of the Book of Mormon in that we don’t know their mtDNA affiliation. Lehi’s group could have belonged either to a typical Middle Eastern lineage or to a rare one, including some that might have had a close Asian affinity. To elucidate this point, I use my own Y chromosome (Ycs) haplogroup as an example. As explained earlier, Ycs is a uniparental marker that, similarly to mtDNA, can be traced along one specific family tree branch (in this case the direct paternal line) and for the most part it does not recombine with the other chromosomes (Figure 2). Ycs haplotypes can also be grouped in a large phylogenetic tree based on common characteristics that in most cases can be associated with specific geographic regions. I was born and raised in Italy and can trace my paternal ancestry back several generations to the mid-17th century AD. However, my Ycs belongs to haplogroup C, which has a frequency in Southern Europe of less than 0.05%. Haplogroup C is mostly found in East Asia with a branch (C4) found among the aborigines of Australia. How did haplogroup C become part of my paternal ancestry? One possibility is that it could be a remnant from an ancient military expansion from the East (e.g. Mongols or Huns) that reached to northern Italy. With my three sons, we contribute four instances of this particular Ycs haplotype in the state of Utah, where we currently reside. If someone took a survey of Italians in Utah with the purpose of reconstructing the typical Italian genetic composition, they would include my three sons and me as part of that count. This would contribute a higher than normal haplogroup C frequency found among Utah-Italians that would in turn provide a different scenario from the one observed in Italy. What if I was the first and only Italian that migrated to Utah? What was considered a rare lineage in the source population (Italy) becomes the totality of the Ycs lineages for the same population in Utah. By looking at these data one may reach the incorrect conclusion that Italians are paternally related to eastern Asian populations. This is a direct result of another principle of population genetics, the founder effect. So, what was Lehi’s family mtDNA contribution to the modern Native American population? It is not possible to know the mtDNA affiliation that was brought with them to America—either a typical Middle Eastern haplogroup, or a rare, even a potential Asian-like subclade.33
The same founder effect process can be observed with mtDNA lineages that are traditionally associated with the Paleo-Indians who arrived in the Americas most likely via Beringia between 12-20,000 years ago. Haplogroups A2, B2, C1, and D1 are the most common mtDNAs found in Native Americans (~95% of the population), but they are not the only and most common mtDNA lineages found in Northeast Asia. For one thing, there are no A2, B2, C1, or D1 lineages in that part of the world (with few exceptions -e.g., subclade C1a, found only in Asia and not in the Americas).34 These four branches of the mtDNA world tree are exclusively found in the Americas and have been separated from all other lineages long enough to develop their own specific mutational motifs. Secondly, a survey of North Asian mtDNA lineages would reveal a much more diverse distribution and variety of mtDNA haplogroups—not a 95% frequency of Asian lineages belonging to subbranches of the roots A, B, C, and D. What happened to the other Asian lineages? Why are they not found in the Americas, too? Genetic drift and founder effect are again the answer. What we observe today in the Western Hemisphere are the surviving lineages that Paleo-Indians brought with them to the Americas at the time of the Last Ice Age. The other lineages were simply lost in the process.
What about Haplogroup X?
Although the majority (~95%) of mtDNA lineages surveyed to date in the Americas belong to a subclade of one of the four pan-American haplogroups (A2, B2, C1, and D1) having Asian affinity, this does not mean that all the pre-Columbian lineages are of Asian origins. One exception is the less-common and geographically-limited haplogroup X. The presence of haplogroup X in the Americas has caused no small perplexity among scientists studying Native American origins. Some of the questions researchers have been trying to address are:
- How does haplogroup X differ from the other pan-American haplogroups with Asian affinity?
- What are its origins?
- Where else is it found in the world?
- What route did it follow to the Americas and how long ago did it arrive there?
With regard to the Book of Mormon and DNA debate, haplogroup X has also played an interesting role at both ends of the spectrum in challenging or defending the historicity of the Book of Mormon. On one end are those who criticize the Book of Mormon based on the DNA data. Conversely, there are some within the LDS faith claiming that the presence of haplogroup X in the Americas supports the truthfulness of the Book of Mormon. The mutually exclusive reasoning of these two factions can be summarized as follow:
- Against: Like other pan-American clades, haplogroup X is of Asian origin arriving to the Americas via Beringia (the landmass that connected north-east Siberia with modern day Alaska during the Last Ice Age). This migration took place more than 10,000 years ago, long before Israel ever existed.
- In favor: Haplogroup X is of Near Eastern origin and its presence in the Americas represents the surviving legacy of Lehi and his family arriving to the Western Hemisphere ~2,600 year ago.
There are probably as many gradients between these two views as people trying to address this specific topic. However, these two points summarize most of the issues surrounding haplogroup X and the proposed association with the historicity of the Book of Mormon.
Following the discovery of the first, more common, Native American mtDNA haplogroups in the early 1990s (originally termed A, B, C, and D and later renamed A2, B2, C1, and D1 to distinguish them from their Asian “cousins”), a fifth haplogroup was identified in 1996 by Forster and colleagues and named haplogroup X (not to be confused with the X chromosome).35 Contrary to nearly all the world haplogroups, it is not geographically confined, but it is found at low frequency among several populations: Europeans, Africans, Asians, Middle Easterners, and Native Americans. A number of studies following the initial identification of haplogroup X among Amerindians confirmed its presence in the Western Hemisphere,36 its variance from the X lineages found in Eurasia and Africa, and its geographic distribution confined to northern North America.37 The Native American clade of haplogroup X is known as X2a to differentiate it from the forms of haplogroup X found in Northern Africa and Eurasia. The root of this lineage is characterized by the diagnostic control region transition C16278T and the specific X2a subclade includes also mutations at A200G and G16213A.38
As already discussed, the pan-American haplogroups A2, B2, C1, and D1, comprising ~95% of today’s Native American mtDNA lineages, are clearly nested within a tree of East Asian haplogroups, thus suggesting an Asian origin followed by a Beringian migration—which led to the differentiation of Paleo-Indian lineages from the ancestral Asian ones—for these haplogroups. It is important to note that these ancestral lineages are not found in northeast Asia, as there are no such things as haplogroup A, B, C, and D there today. A, B, C, and D differentiated in ancient south Asia during the early expansion of anatomically modern humans tens of thousands of years ago (a geographic region that is not any closer to Beringia than is the Middle East). Lineages found today in central and northeast Asia (e.g., A5, B4a, C4, and D4e, just to name a few) are considered “cousins” but are not ancestral to the American A2, B2, C1, and D1 haplogroups (Figure 1).
For years scientists struggled in identifying a possible Asian source for haplogroup X that could explain its presence in the Western Hemisphere. Different theories were postulated, including a possible northern Atlantic migration along the ice cap that connected northern Europe to northern America during the Last Ice Age. This unpopular theory—referred to as the Solutrean hypothesis—was supported by archeological discoveries revealing the presence of a similar technology in both continents arising at about the same time period.39
Early studies were limited to the sequence of a few hundred bases from the control region and therefore were not able to provide the level of resolution necessary to assess the phylogenetical relationship between American and Eurasian X lineages. This is particularly relevant in light of the fact that, initially, haplogroup X could not be found in Asia and therefore there was even more uncertainty regarding its origin and migration route to the Western Hemisphere. Did haplogroup X come from Europe via the glaciated northern Atlantic, or did it follow the same Beringian route as the other Native American haplogroups? If the latter was the case, why was it not found in northern Siberia or eastern Asia?
Scientists began looking for the presence of haplogroup X in other areas of Asia and eventually were able to find it in a small percentage of the Altai population, on the northern border of Mongolia. In 2001, Derenko and colleagues published a paper in which they reported the Altaian haplogroup X haplotypes (control region only) together with Eurasian and American X lineages and suggested that their intermediary position could possibly represent the population source for haplogroup X in northern North America.40 Its absence in north Siberian populations could be explained by a rapid expansion or by its disappearance due to genetic drift. However, when the same data were analyzed at a higher level of resolution—that of complete mtDNA sequences—and compared to other X haplotypes, it became evident that the Altaian mtDNA cluster (called X2e) was considerably younger than the Native American X2a. Therefore, the Asian branch of X was not ancestral to the Amerindians X2a, but it certainly could be a sister clade derived from a common, now disappeared, Asian ancestor. The authors suggested that the Altaian X’s were the result of a secondary, more recent migratory event, possibly from the Caucasus region,41 leaving the question about the origin of Native American X2a unanswered. The authors concluded their research by stating that “phylogeography of the subclades of haplogroup X suggests that the Near East is the likely geographical source for the spread of subhaplogroup X2.”42 Interestingly, they identified a sample from Iran that shared a single, fairly conserved coding region mutation with the Native American X2a cluster: “We surveyed our Old World haplogroup X mtDNAs for the five diagnostic X2a mutations [A200G and G16213A in the control region and A8913G, A12397G, and T14502C in the coding region] and found a match only for the transition at nucleotide position A12397G in a single X2* sequence from Iran. In a parsimony tree, this Iranian mtDNA would share a common ancestor with the Native American clade.”43 However, the authors suggested that this could have been a case of IBS (identical by state, where shared mutations in different populations arise by chance in a parallel manner with no common ancestor), rather than IBD (identical by descent, where shared mutations that exist in different populations originated from a common ancestor). In other words, since they could not explain how the Iranian sample could possibly cluster with the Native American X2a lineages, they deduced that the common mutation was simply due to chance and not because of a more recent common ancestry. It wasn’t until 2008, with the publication of two papers on Middle Eastern populations, that more light on the origin of haplogroup X was shed.44 One of them focused on the Druze population of northern Israel.
The Druze are a religious group—originating as an off-shoot of Islam—numbering approximately one million people living principally in Syria, Lebanon, Israel, and Jordan. The authors of the paper on Druze mtDNAs observed that most of the X lineages found elsewhere (Africa, Europe, and Asia) were also detected among the Druze, thus suggesting that they could indeed have been the source population for the spreading of haplogroup X throughout the world. Although no Native American X2a mtDNAs were observed among these people, the Altaian X2e was one of the haplotypes that the researchers identified, thus confirming a more recent migratory event that led to the presence of X2e in modern-day south Siberia. Additionally, in 2009 a paper describing mtDNA lineages from Egyptian nomads revealed a small number of haplotypes carrying the same diagnostic coding region mutation shared by the Native American X2a samples and the one from Iran reported in 2003.45 This finding may support the conclusion that such a mutation may indeed be ancestral to all of these samples leaving the door open to future studies that may contribute additional knowledge about a possible more recent relationship—when compared to the pan-American and Asian haplogroups—between Amerindian X2a and Middle Eastern haplotypes.
This brief summary of studies focusing on the origin and diffusion of haplogroup X contains some of the details that have been used in the Book of Mormon debate over the past few years. Some Mormon scholars welcomed the association between a small group of Native American lineages and people of the Middle East as the genetic evidence that indeed there was a group of seafaring Israelites that arrived in the Americas within the last couple thousand years. On the other hand, critics of the Book of Mormon dismissed this possibility by first referring to the presence of haplogroup X among the Altaians (and therefore supporting the scenario that this lineage followed the same Beringian route to the New World at the same time as the other pan-American mtDNAs).46 As already discussed, this first hypothesis is now challenged by data from complete mtDNA sequences that exclude the Asian X lineage as being the potential ancestor to the American one. A second criticism with regard to a possible association between Book of Mormon people and the X2a lineage is based on the current coalescent age of haplogroup X2a, as well as findings based on ancient DNA studies supporting a longer presence of this lineage in the Americas—close in time to the origin of other Native American haplogroups—and therefore predating the events recorded in the Book of Mormon.
The first issue deals with the age estimate based on modern DNA. There are currently five molecular clocks that have been proposed to calculate the age of mtDNA lineages using data from coding regions or complete sequences.47 Only one of these mutation rates is based on the complete mtDNA genome (both control and coding regions), providing an age estimate for X2a (12,800 ± 6,600 years ago), which is similar to the four pan-American haplogroups.48 The ages obtained using the other molecular clocks are fairly comparable. The X2a distribution limited to northern North America strongly suggests a separate migratory event from Beringia through the ice-free corridor that was open between the Cordilleran and Laurentide glaciers at the end of the Last Ice Age.49 In order for X2a to fit within Book of Mormon chronology, the currently accepted molecular clocks would need considerable re-calibration,50 or other samples from the Old World carrying additional mutations shared with the Native American X2a would be needed. Neither of these two scenarios is currently likely, and neither may ever become a possibility to conclusively demonstrate a link between X2a and Lehi’s party.
The discussion of the X haplotype illustrates the challenges encountered when attempting to reconstruct genetic scenarios from modern populations compatible with the Book of Mormon timeline and expected source population. Based on the molecular clocks currently used by the scientific community, it would be nearly impossible to distinguish a Eurasian lineage that arrived 2,600 years ago from those brought by Europeans after the discovery of America’s double-continent, simply because there would not have been enough time for these lineages to differentiate enough to allow discernment of pre-Columbian from post-Columbian admixture. The only truly testable hypothesis that unequivocally evaluates the historicity of the Book of Mormon from a molecular perspective would be to know the actual genetic profiles of Lehi’s group, identify them in the modern Native American populations, and find exact matches in samples from their Middle Eastern area of origin (assuming that genetic drift and population bottlenecks had not obliterated the genetic signal over time). Unfortunately, as already discussed, to attribute a particular genetic profile to Lehi’s group would be pure speculation, making the testing of this hypothesis impossible.
With regard to ancient DNA studies exploring the presence of X2a in ancient times in the Americas, there are three papers addressing this issue.51 As previously discussed, X2a is defined by five diagnostic mutations (two control and three coding region transitions). However, researchers of ancient mtDNA have been limited to a small segment of the control region and therefore their classification of mtDNA lineages from ancient samples was based solely on one basal mutation for the root of haplogroup X (C16278T). This mutation is shared by all the X lineages worldwide, and is also a mutational hotspot—a nucleotide position that recurrently mutates in the world mtDNA phylogeny. According to a recent publication surveying 2,000 complete mtDNA sequences, C16278T was the twelfth most common mutation observed.52 Using this single site as the diagnostic mutation to place ancient samples into the X haplogroup already poses a serious limitation to the accuracy of such inferences. Two of the three papers in question pre-date the era of gold standards for ancient studies, which already constitutes a potential concern in confidently accepting the quality of their results and subsequently of the conclusion derived from such analyses.
The first paper dealt with a burial site in Windover, Florida, where 176 individuals were identified and recovered. The site was carbon-dated at approximately 7-8,000 years ago and a short section of the mtDNA control region (166 bases from position 16151 to position 16317) was sequenced for fourteen individuals. Two of the specimens analyzed yielded the recurrent mutation C16278T, which is also diagnostic for the whole X haplogroup. However, neither of them reported the common G16213A transition, which would have been found within the range that was sequenced. Additionally, the mutations of these two haplotypes are not sufficient to allow an unambiguous assignment to either haplogroup X2a or any of the other pan-American haplogroups. The authors admitted that “given the limited number of Windover samples currently analyzed and the restricted length of mtDNA sequences analyzed any inference regarding Windover structure or its relationship to contemporary Amerind groups is necessarily tentative.”53
The second paper dealing with haplogroup X2a from ancient DNA was based on specimens retrieved from a Native American cemetery at the Norris Farm site in Illinois. Archeologists classified the site as being part of the Oneota culture and dated it at about 1,000 years ago, a timeframe that would fit with Book of Mormon chronology. DNA was extracted successfully from 108 individuals, but only 52 of them were sequenced for a segment of the mtDNA control region (353 bases, from position 16056 to position 16409). Nearly all haplotypes were assigned to one of the four major pan-American haplogroups, with the exception of two that bore the X-specific C16278T transition and none of the A2, B2, C1, and D1 diagnostic mutations. However, as with the previous paper, both samples are missing mutation G16213A found in nearly all modern-day X2a samples.
Contamination, post-mortem damage, parallel or back mutations, and misclassification due to the limited data available could be some of the possible explanations for the presence of C16278T and the absence of G16213A, which resulted in the inability to confidently determine the existence of haplogroup X in the ancient burial sites described in these first two papers.54 Currently, the first convincing evidence of haplogroup X in pre-Columbian America comes from a 2002 study reporting ancient DNA data from a ~1,340-year-old burial site on the Columbia River near Vantage, Washington.55 It is not excluded that future studies—including a more detailed and controlled analysis of the samples from the 8,000-year-old Windover burial site—may eventually confirm the presence of haplogroup X in pre-Book of Mormon America. It is also possible that the specimens analyzed could belong to a rarer or extinct X subclade, distantly related to the more common X2a found in the modern native population of northern North America, as demonstrated by the recently discovered X2g lineage found in an Ojibwa sample.56
What about other mtDNA lineages found in the Americas?
Molecular anthropologist Ted Schurr addressed the issue of Amerindian lineages not belonging to the classical pan-American haplogroups by stating that “various studies have also revealed a high frequency of ‘private haplotypes’ in individual populations or groups of related Amerindian tribes. These patterns reflect the role that genetic drift and founder effects have played in the stochastic extinction and fixation of mtDNA haplotypes in Native American populations. A number of haplotypes not clearly belonging to these five maternal lineages have been also detected in different Native American groups. These ‘other’ mtDNAs have often been considered additional founding haplotypes or haplogroups in New World populations. However, most have since been shown to be derivatives of haplogroups A-D that have lost diagnostic mutations. The remainder appears to have been contributed to indigenous groups through nonnative admixture. In addition, the ‘other’ mtDNAs detected in archeological samples may have resulted from contamination with modern mtDNAs, or were insufficiently analyzed to make a determination of their haplogroup status.”57
The process of discovering additional pre-Columbian lineages in the Americas is somewhat limited by the pre-conceived notion that if a lineage does not fit with the classical Native American haplotypes, it is most likely the result of a recent migratory event from the Old World. For example, a 1999 study on the Cayapa tribe of Ecuador revealed a number of lineages that did not fit with the five known Native American haplogroups.58 Although the authors believed it could have been a newly identified pre-Columbian lineage and called it the “Cayapa haplotype,” others dismissed it as a possible case of European mtDNA introgression.59 However, it was only when mtDNA data became available from the ~10,000 year old Alaskan skeleton described earlier that the Cayapa haplotype was confirmed as a genuine pre-Colombian novel lineage.60 From the initial four Amerindian mtDNA haplogroups discovered in the early 1990s, at least thirteen Native American founding lineages are currently catalogued and it is very likely that more will be identified in future studies.61 Additionally, detailed studies based on complete mtDNA sequences of haplotypes belonging to peculiar branches of the four pan-American haplogroups may reveal interesting distribution patterns reflecting novel migratory events that could not be detected based on control region data only.
What about Ycs and Autosomal DNA Studies?
The purpose of this essay is to provide an updated review of mtDNA research on Native American populations in light of the Book of Mormon debate. In the interest of space, it is not feasible to discuss in detail data from additional genetic systems, but a brief review of findings will be highlighted.
The Ycs data produced to date is still fairly scarce and there is much work to be done to fully investigate the history of the Ycs in Native American populations. Future studies will need to test many more samples at a higher level of resolution in order to achieve a greater dissection and understanding of Amerindian Ycs haplogroups. Additionally, while autochthonous mtDNA lineages are still found abundantly both among indigenous and mixed American populations,62 the European male contribution to the Native American gene pool was devastating, in terms of preserving the native American genetic signal. The genetic bottleneck experienced in Ycs lineages was tenfold more severe than its female counterpart, thus making studies based on this uniparental paternal marker far less informative in elucidating Native American genetic history.
With regard to autosomal DNA, the genetic reshuffling that occurs at each generation creates serious limitations in the ability to trace specific ancestral lineages unequivocally. When compared to the uniparental markers Ycs and mtDNA, the study of autosomal DNA is far more complex and less forthcoming in straightforward interpretation. Recent technological advances now allow for the testing of up to one million polymorphic autosomal sites for an individual, providing an unprecedented level of resolution in characterizing an individual’s genetic profile. From such an abundance of data, statistical analysis can give the estimated percentage of an ancestral population’s contribution to an individual’s genetic makeup. This can provide a picture of genetic influences that may have come in from other populations but that may not be reflected in the strictly maternal or paternal ancestral lineage. However, with regard to the Book of Mormon discussion, autosomal DNA inheritance is subject to the same population forces as other genetic systems (genetic drift, genetic bottleneck, and founder effect), and considering the likely demographic scenario of the Book of Mormon (i.e., a small group of Old World migrants mixing with a large population of ancient Asian origins), the probable findings of autosomal studies are unlikely to contradict results already achieved with mtDNA and Ycs data. Native American Ycs, mtDNA, or autosomal DNA data analyzed will likely continue to produce a predominantly Asian signal.
A recent study based on a small section of DNA found on chromosome 9 had the objective of determining the origin and number of Paleo-Indian migrations. Based on their analysis, the authors concluded that “all modern Native Americans […] trace a large portion of their ancestry to a single founding population that may have been isolated from other Asian populations prior to expanding into the Americas.”63 This study was recently mentioned as further demonstration that conclusions by critics of the Book of Mormon in the past are indeed correct, based on the fact that the study purportedly reported that all Native American populations and all individuals analyzed carried the same autosomal polymorphic mutation found also in Asian populations.64 Book of Mormon opponents, however, disregard several key points in their arguments. First, as already discussed, the presence of indigenous populations of Asian origins prior to the arrival of Book of Mormon people does not affect the historicity of the book itself. These autosomal findings are in line with what is already known about Native American populations, and do not change arguments, already presented, that propose that Book of Mormon events are compatible with the Asian-dominated genetic landscape found in Native Americans today. Population bottleneck, founder effect, genetic drift, and other population-altering forces affect all genetic systems, including autosomal DNA. It would not be unusual to expect that the small autosomal contribution of Lehi and his followers could be lost over time when mixing with an already established population of Asian origin. Additionally, the authors concluded that “a large portion” and not all the Native American ancestry can be traced to a single population with Asian affinity. A further important point comes from the idea of hypothesis construction. This research was not designed to identify a possible presence of Western Eurasian-specific markers in the Amerindian populations, and thus it is not surprising that none was found.
Of greater relevance to the debate about possible subsequent migrations to the Western Hemisphere, besides those that occurred in the post-Last Ice Age era is a recent study published in the prestigious journal Nature. The authors reported autosomal DNA data that was successfully sequenced from hair belonging to a well-preserved 4,000-year-old Saqqaq individual discovered in Greenland.65 This research contributed greatly to the current understanding of events that led to the peopling of the Americas, as the authors concluded that the genetic make-up of the ancient Saqqaq individual was very different from that of Inuit or other Native American populations. Instead, he was closely related to Old World Arctic populations of the Siberian Far East, being separated from them by approximately 200 generations (roughly 5,500 years). These data suggest a distinctive and more recent migration across Beringia by a group of people that were not related to the ancestors of modern-day Native Americans, who arrived on the American continent nearly ten thousand years earlier. As the senior author emphasized, the lack of genetic continuity between the ancient Saqqaq individual and the modern population of the New World Arctic stands as a witness that other migrations could have taken place that left no contemporary descendants.66 In commenting about the findings of this project, population geneticist Marcus Feldam from Stanford University said that “the models that suggest a single one-time migration are generally regarded as idealized systems, like an idealized gas in physics, but there may have been small amounts of migrations going on for millennia. Just because researchers put a date on when ancient human crossed the Bering Bridge, that doesn’t mean it happened only once and then stopped.”67
The Book of Mormon is not a volume about the history and origins of all American Indians. A careful reading of the text clearly indicates that the people described in the Book of Mormon were limited in the recording of their history to events that had religious relevance and that occurred in relative close proximity to the keepers of the annals.
The fact that the DNA of Lehi and his party has not been detected in modern Native American populations does not demonstrate that this group of people never existed, nor that the Book of Mormon cannot be historical in nature. The absence of evidence is not evidence of absence. Further, the very idea of locating the genetic signature of Lehi’s family in modern populations constitutes a truly un-testable hypothesis, as it is not possible to know the nature of their genetic profiles. Without knowing the genetic signature to be located, any attempt at researching it will unavoidably result in further assumptions and non-testable hypotheses. What were the characteristics of Lehi’s DNA and the DNA of those who went along with him? What haplogroup(s) did they belong to? We will never know. Yet this key point seems lost on those who insist on using genetic evidence as a means to validate or refuse the Book of Mormon as an historical narrative. Attempting to make such conclusions is a miscarriage of logic comparable to that of a hypothetical crime scene from which no DNA could be retrieved for the individual who committed the crime. Yet nevertheless, in order to solve the case, the DNA of thousands of people living in the area surrounding the crime scene is collected and analyzed, thus creating a comprehensive database of all these people. Will the database include the DNA signature of the criminal? If so, how could the perpetrator be identified among the thousands of others? Similarly, would a database composed of thousands of Native American DNA samples provide the necessary evidence to validate the existence of a small group (perhaps as few as two mtDNA haplotypes) that migrated from the Old World and settled somewhere in the Americas? Conversely, could haplogroup X be undoubtedly inferred as the ultimate proof of the genetic legacy this group left, without ever knowing their actual original DNA signature? MtDNA is a powerful tool in reconstructing the history of our race, as demonstrated by the numerous publications that have been produced over the past two and a half decades. However, as has been amply demonstrated, knowing a great deal about the genetic composition of modern-day Native American populations does not give conclusive evidence of the validity or the implausibility of the Book of Mormon’s historicity.
An additional caveat is the lack of professional training in population genetics by those promoting a supposed discrepancy between the genetic evidence and the Book of Mormon account. Some of them claim that their conclusions are strongly supported by trained experts who have been consulted for unbiased opinions about this particular matter.68 This should raise some concerns, though, since it is fairly obvious that most people outside of the circle of Mormonism have very limited knowledge of the Book of Mormon and its contents. As a further counterpoint to the critics’ arguments, these experts seem to be in agreement that DNA lineages from a small Old World group migrating to an already heavily populated American continent would disappear.69 Moreover, it is also noteworthy that what these scientists know about what “Mormons believe” has been provided mainly as one-sided background information from the critics themselves. To offer a personal anecdote, I have been asked by scientist colleagues about the Book of Mormon and the DNA issue on several occasions. After providing a simple summary by explaining the possibility that the DNA lineages could have been lost due to genetic drift, since the number of individuals involved was probably fairly small compared to the size of the Amerindian population, or that it is not possible to distinguish them from post-Columbian admixture simply because 2,600 years is not enough time for Book of Mormon mtDNA to differentiate them from their Eurasian counterparts, they indicated that they were not convinced that this was what Mormons believe. These personal experiences give context for evaluating “genuine expert’s opinions,” based on what the critics may have shared with them as background information regarding the Book of Mormon and the beliefs of the LDS Church. Ultimately, the critics’ arguments only hold up when they themselves prescribe what it is that Mormons believe. Since neither the Book of Mormon nor LDS doctrine indicates that all Native Americans descend from the Book of Mormon people, their arguments are on weak footing at the outset.
In light of the information provided in this essay, it is evident that the work of reconstructing the history of Native American populations using molecular data is still under way. Some general answers are known, and others are questioned, while research is underway for many more questions. The genetic evidence of the peopling of the Americas is not fully understood and it has evolved substantially over the past two decades. DNA research, and particularly mtDNA data, has been produced in great abundance during this time period and has provided an initial glimpse into the history and pre-history of the indigenous people of the Western Hemisphere. This is truly an exciting time to study the genetic history of Native Americans, as there is much yet to be understood. For example, how is the high frequency of haplogroup B in South-East Asia and western South America reconciled with its rarity in the native populations of North Siberia and Alaska? The scarcity of archeological evidence for human settlements on either site of the Bering Strait provides a degree of intrigue, considering that mainstream scientists currently accept Beringia as the likely refugium for Paleo-Indians during the Last Ice Age, leaving open the possibility for alternative routes into the Americas.70 MtDNA is doubtless a powerful tool to reveal details about the expansion processes that led to the colonization of the world, including America’s double-continent. However, it is not well suited as the ultimate tool to assess the historicity of religious documents like the Book of Mormon and the Bible. If the DNA of Lehi and his family cannot be confidently detected in the modern Amerindian population, does it mean that they never existed? The principles of this question can be further extrapolated to other religious scenarios. Can we use DNA to unquestionably prove that the great biblical patriarchs – Abraham, Isaac, and Jacob – ever existed? What were their and their descendants’ mtDNA haplotypes? What about the other great Old Testament figures, such as Joseph of Egypt, Moses, and Isaiah? Can we prove that Jesus Christ lived through DNA? The New Testament mentions that Jesus had brothers and sisters71 through whom Mary’s mtDNA could have been transmitted to future generations (and if not through Mary, perhaps through some of her female relatives). Where is their DNA in today’s population? Would it be acceptable to conclude that these are fictional historical figures and the biblical text a hoax because of the lack of genetic evidence? As I already commented on another occasion: “I find no difficulties in reconciling my scientific passion about Native American history with my religious beliefs. I am not looking for a personal testimony of the Book of Mormon in the double helix. The scientific method and the test of faith are two strongly connected dimensions of my existence, working synergistically in providing greater understanding, knowledge, and from time to time even a glimpse into God’s eternal mysteries.”72 Anyone using DNA to ascertain the accuracy of historical events of a religious nature – which require instead a component of faith – will be sorely disappointed. DNA studies will continue to assist in reconstructing the history of Native American and other populations, but it is through faith that we are asked to search for truth in holy writings.73
1 Ugo A. Perego is Senior Researcher and Director of Operations at the Sorenson Molecular Genealogy Foundation in Salt Lake City, Utah. He recently received a PhD in Human Genetics from the University of Pavia, Italy, with an emphasis on mitochondrial DNA analysis applied to the study of populations. The author is grateful to the following individuals for commenting on this manuscript: Dr. Alessandro Achilli (University of Perugia, Italy), Jayne E. Ekins, Diahan Southard, and Dr. Scott R. Woodward (Sorenson Molecular Genealogy Foundation, USA), Professor Antonio Torroni (University of Pavia, Italy), and Dr. Amy Williams (Harvard Medical School, USA).
2 Dennis H. O’Rourke, ‘Human Migrations: The Two Roads Taken’, Current Biology 19 (2009), R203—R204.
3 2 Kings 17:6
4 Michael Crawford, The Origins of Native Americans: Evidence from Anthropological Genetics (Cambridge—Cambridge University Press, 1998).
5 Geraldine Barnes, Viking America: The First Millennium (Suffolk—St. Edmundsbury Press Ltd, 2001). Note that no genetic contribution from Vikings has been detected to date in the modern Native American population. Either they kept to themselves and were not welcomed by native groups, or their DNA has not yet been identified in contemporary Amerindians.
6 Antonio Torroni and others, ‘Asian Affinities and Continental Radiation of the Four Founding Native American mtDNAs’, American Journal of Human Genetics 53 (1993), 563—590; Alessandro Achilli and others, ‘The Phylogeny of the Four Pan-American MtDNA Haplogroups: Implication for Evolutionary and Disease Studies’, PLoS One 3 (2008), e1764.
7 For a summary of the principal Book of Mormon New World geography theories, see http://en.fairmormon.org/Book_of_Mormon/Geography/New_World (accessed November 2009).
8 Carrie A. Moore, ‘Debate Renewed with Change in the Book of Mormon Introduction’, Deseret Morning News (available at http://www.deseretnews.com/article/1,5143,695226008,00.html – accessed December 2009).
9 Conference Reports (April 1929), 15—16.
10 See for example John L. Sorenson ‘When Lehi’s Party Arrived in the Land, Did They Find Others There?’, Journal of Book of Mormon Studies 1 (1992), 1—34; John L. Sorenson and Matthew Roper, ‘Before DNA’, Journal of Book of Mormon Studies 12 (2003), 6—23; Blake T. Ostler, ‘DNA Strands in the Book of Mormon’, Sunstone (May 2005), 63—71.
11 Examples of Book of Mormon criticisms based on DNA evidence are found in Simon G. Southerton, Losing a Lost Tribe: Native Americans, DNA, and the Mormon Church (Salt Lake City—Signature Books, 2004); Thomas W. Murphy, ‘Lamanite Genesis, Genealogy, and Genetics’, in American Apocrypha: Essays on the Book of Mormon eds. Dan Vogel and Brent Metcalfe (Salt Lake City—Signature Books, 2002); Brent L. Metcalfe, ‘Reinventing Lamanite Identity’, Sunstone(March 2004), 20—25. A collection of LDS views on the general issue of DNA and Book of Mormon are found in The Book of Mormon and DNA Research ed. Daniel C. Peterson (Provo—The Neal A. Maxwell Institute for Religious Scholarship, 2008). Arguments supporting DNA evidence in favor of Book of Mormon historicity are summarized in Rod L. Meldrum, Rediscovering the Book of Mormon Remnant through DNA (New York—Digital Legend Press, 2009).
12 Ugo A. Perego, Jayne E. Ekins and Scott R. Woodward, ‘Mountain Meadows Survivor? A Mitochondrial DNA Examination’, Journal of Mormon History 32 (Fall 2006), 45—53.
13 Stephen Anderson and others, ‘Sequence and Organization of the Human Mitochondrial Genome’, Nature 290 (1981), 457—465.
14 Richard M. Andrews and others, ‘Reanalysis and Revision of the Cambridge Reference Sequence for Human Mitochondrial DNA’, Nature Genetics 23 (1999), 147.
15 Marianne Schwartz and John Vissing, ‘Paternal Inheritance of Mitochondrial DNA’, New England Journal of Medicine 347 (2002), 576—580.
16 Also called the hypervariable or D-loop region.
17 Sometimes referred to as HVR1, HVR2, and HVR3.
18 Antonio Torroni and others, ‘Native American Mitochondrial DNA Analysis Indicates that the Amerind and the Nadene Populations were Founded by Two Independent Migrations’, Genetics 130 (1992) 153—162; Antonio Torroni and others, ‘mtDNA and Y-chromosome Polymorphisms in Four Native American Populations from Southern Mexico’, American Journal of Human Genetics 54 (1994), 303—318; Antonio Torroni and others, ‘Mitochondrial DNA “Clock” for the Amerinds and Its Implications for Timing Their Entry into North America’, Proceedings of the National Academy of Sciences 91 (1994), 1158—1162; Peter Forster and others, ‘Origin and Evolution of Native American MtDNA Variation: A Reappraisal’,American Journal of Human Genetics 59 (1996), 935—945; just to cite a few.
19 Antonio Torroni and others, ‘Do the Four Clades of the MtDNA Haplogroup L2 Evolve at Different Rates?’, American Journal of Human Genetics 69 (2001), 1348—1356.
20 Luísa Pereira and others, ‘The Diversity Present in 5140 Human Mitochondrial Genomes’, The American Journal of Human Genetics 84 (2009), 628—640; Mannis van Oven and Manfred Kayser, ‘Updated comprehensive phylogenetic tree of global human mitochondrial DNA variation’ Human Mutations 30 (2009) E386—E394 (http://www.phylotree.org – accessed November 2009). As of November 5, 2009, the publicly accessible GenBank database contained 6,571 complete mtDNA sequences, but the number of those belonging to known Native American haplogroups still suffers from significant underrepresentation (http://www.ncbi.nlm.nih.gov/nuccore – accessed November 2009).
21 Alessandro Achilli and Ugo A. Perego, ‘Mitochondrial DNA: A Female Perspective in Recent Human Origin and Evolution’, in Origins as a Paradigm in the Sciences and in the Humanities, eds. Paola Spinozzi and Alessandro Zironi (in press).
22 Torroni, (1993).
23 Agnar Helgason and others, ‘A Population-wide Coalescent Analysis of Icelandic Matrilineal and Patrilineal Genealogies: Evidence for a Faster Evolutionary Rate of mtDNA Lineages than Y Chromosomes’, American Journal of Human Genetics72 (2003), 1370—1388.
24 Simon Southerton, ‘Answers to Apologetic Claims about DNA and the Book of Mormon’ (http://www.signaturebooks.com/excerpts/Losing2.htm—accessed November 2009).
25 http://en.wikipedia.org/wiki/Genetic_drift (accessed August 2009).
26 Crawford, (1998).
27 Beth A. S. Shook and David G. Smith, ‘Using Ancient mtDNA to Reconstruct the Population History of Northeastern North America’, American Journal of Physical Anthropology 137 (2008), 14—29.
28 Amy Harmon, ‘DNA Gatherers Hit Snag: Tribes Don’t Trust Them’, The New York Times (http://www.nytimes.com/2006/12/10/us/10dna.html?_r=2&oref=slogin&pagewanted=all—accessed December 2009).
29 Alan Cooper and Hendrik N. Poinar, ‘Ancient DNA: Do It Right, or Not at All’, Science 289 (2000), 530—531.
30 Adrian W. Briggs and other, ‘Targeted Retrieval and Analysis of Five Neandertal mtDNA Genomes’, Science 325 (2009), 318—321; Luca Ermini and others, ‘Complete Mitochondrial Genome Sequence of the Tyrolean Iceman’, Current Biology 18 (2008), 1687—1693.
31 Brian M. Kemp and others, ‘Genetic Analysis of Early Holocene Skeletal Remains from Alaska and Its Implication for the Timing of the Peopling of the Americas’, American Journal of Physical Anthropology 132 (2007), 605—621.
32 Ugo A. Perego and others, ‘Distinctive Paleo-Indian Migration Routes from Beringia Marked by Two Rare MtDNA Haplogroups’, Current Biology 19 (2009) 1—8. A single haplotype sharing part of the D4h3 motif was also identified in the province of Shandong, China, out of more than ten thousand Asian mtDNAs.
33 Although some information is available about the ancestry of Lehi and Ishmael, we know nothing about the origins of Sariah and Ishmael’s wife, who were responsible for passing their mtDNA to future generations.
34 Erika Tamm and others, ‘Beringian Standstill and Spread of Native American Founders’, PloS One 9 (2007), e829.
35 Forster, (1996).
36 Michael D. Brown and others, ‘MtDNA Haplogroup X: An Ancient Link Between Europe/Western Asia and North America?”, American Journal of Human Genetics 63 (1998), 1852—1861; David G. Smith and others, ‘Distribution of MtDNA Haplogroup X Among Native Americans’, American Journal of Physical Anthropology 110 (1999), 271—284.
37 Rosaria Scozzari and others, ‘MtDNA and Y Chromosome-Specific Polymorphisms in Modern Ojibwa: Implications about the Origin of Their Gene Pool’, American Journal of Human Genetics 60 (1997) 241—244; Perego, (2009).
38 Achilli, (2008); Perego, (2009).
39 Dennis Stanford and Bruce Bradley, ‘Ocean Trails and Prairie Paths? Thoughts about Clovis Origins’, in The First Americans: The Pleistocene Colonization of the New World, ed. NG Jablonski (San Francisco—Academy of Science, 2002); Bruce Bradley and Dennis Stanford, ‘The North Atlantic Ice-edge Corridor: A Possible Paleolithic Route to the New World’, World Archaeology 36 (2004), 459—478.
40 Miroslava V. Derenko and others, ‘The Presence of Mitochondrial Haplogroup X in Altaians from South Siberia’, American Journal of Human Genetics 69 (2001), 237—241.
41 Maere Reidla and others, ‘Origin and Diffusion of mtDNA Haplogroup X’, American Journal of Human Genetics 73 (2003), 1178—1190.
44 Shlush and others, ‘The Druze: A Population Genetic Refugium of the Near East’, PLoS One 3 (2008), e2105; Doron M. Behar and others, ‘Counting the Founders: The Matrilineal Genetic Ancestry of the Jewish Diaspora’, PLoS One 3 (2008), e2062.
45 Martina Kujanová and others, ‘Near Eastern Neolithic Genetic Input in a Small Oasis of the Egyptian Western Desert’, American Journal of Physical Anthropology 140 (2009), 336—346.
46 Perego, (2009).
47 For details about the five age estimate models based on complete mtDNA sequences, see Dan Mishmar and others, ‘Natural Selection Shaped Regional MtDNA Variation in Humans’, Proceedings of the National Academy of Sciences 100 (2001), 171—176; Toomas Kivisild and others, ‘The Role of Selection in the Evolution of Human Mitochondrial Genomes’, Genetics 172 (2006), 373—387; Perego, (2009); Pedro Soares and others, ‘Correcting for Purifying Selection: An Improved Human Mitochondrial Molecular Clock’, American Journal of Human Genetics 84 (2009), 740—759; Eva-Liis Loogväli and others, ‘Explaining the Imperfection of the Molecular Clock of Hominid Mitochondria’, PLoS One 4 (2009), e8260.
48 Soares, (2009).
49 Perego, (2009).
50 Supporters of X haplogroup as evidence for Book of Mormon historicity and its geographic setting in northern North America rely on the unpopular molecular clock proposed by a forensic team in 1997, which was based on control region data only (Thomas J. Parsons and others, ‘A High Observed Rate in the Human Mitochondrial DNA Control Region’, Nature Genetics 15 (1997), 363—368).
51 William W. Hauswirth and others, ‘Inter- and Intrapopulation Studies of Ancient Humans’, Experientia 50 (1994), 585—591; Anne C. Stone and Mark Stoneking, ‘MtDNA Analysis of a Prehistoric Oneota Population: Implications for the Peopling of the New World’, American Journal of Human Genetics 62 (1998), 1153—1170; Ripan S. Mahli and David G. Smith, ‘Brief Communication; Haplogroup X Confirmed in Prehistoric North America’, American Journal of Physical Anthropology 119 (2002), 84—86.
52 Soares, (2009). A similar outcome was observed when querying the Sorenson Molecular Genealogy Foundation mtDNA database (http://www.SMGF.org). Out of more than 76,000 samples, C16278T was observed in 8,501 cases in several haplogroups, including all the pan-American lineages.
53 Hauswirth, (1994).
54 Mahli and Smith, (2002).
56 Perego, (2009).
57 Theodore G. Schurr, ‘The Peopling of the New World: Perspectives from Molecular Anthropology’, Annual Review of Anthropology 33 (2004), 551—583.
58 Olga Rickards and others, ‘MtDNA History of the Cayapa Amerinds of Ecuador: Detection of Additional Founding Lineages for the Native American Populations’, American Journal of Human Genetics 67 (1999), 241—260.
59 Schurr, (2004).
60 Kemp, (2007).
61 Achilli, (2008); Perego, (2009); Ugo A. Perego, ‘The Origin of Native Americans: A Reconstruction Based on the Analysis of Mitochondrial Genomes’, PhD Dissertation—Universitá di Pavia, Italy (2009); Ripan S. Mahli and others, ‘Brief communication: Mitochondrial haplotype C4c confirmed as a founding genome in the Americas’, American Journal of Physical Anthropology 141 (2009), 494-497.
62 Alessandro Achilli and others, ‘The Mitochondrial Landscape of Modern Mexico’, 58th Annual Conference The American Society of Human Genetics, Philadelphia, PA, September 11—16, 2008; Alessandro Achilli and others, ‘Decrypting the MtDNA Gene Pool of Modern Panamanians’, 59th Annual Conference The American Society of Human Genetics, Honolulu, HI, October 20—24, 2009. Approximately 80% of the samples tested for the Mexican (n = ~2,000) and the Panamanian (n = ~500) mixed populations belonged to one of the four pan-American haplogroups.
63 Kari B. Schroeder and others, ‘Haplotypic Background of a Private Allele at High Frequency in the Americas’, Molecular Biology and Evolution 26 (2009), 995—1016.
64 ‘A Quantum Leap in DNA Studies’, Signature Books (http://www.signaturebooks.com/news.htm – accessed January 2010).
65 Morten Rasumussen and others, ‘Ancient Human Genome Sequence of an Extinct Palaeo-Eskimo’, Nature 463 (2010), 757—762.
66 Cassandra Brooks, ‘First Ancient Human Sequenced’, (http://www.the-scientist.com/blog/display/57140 – accessed February 2010).
68 See for example the introduction to Simon G. Southerton’s Losing a Lost Tribe, (2004) or Living Hope Ministries’s DNA vs. the Book of Mormon (DVD, 2003).
69 ‘What Happens Genetically When a Small Population Is Introduced into a Larger One?’, Signature Books (http://www.signaturebooks.com/excerpts/DNAAmericas.htm – accessed November 2009). The exact question asked was, “If a group of, say, fifty Phoenicians (men and women) arrived in the Americas some 2,600 years ago and intermarried with indigenous people, and assuming their descendants fared as well as the larger population through the vicissitudes of disease, famine, and war, would you expect to find genetic evidence of their Phoenician ancestors in the current Native American population? In addition, would their descendants be presumed to have an equal or unequal number of Middle Eastern as Native American haplotypes?”
70 Dennis H. O’Rourke and Jennifer A. Raff, ‘The Human Genetic History of the Americas: The Final Frontier”, Current Biology 20 (2010), [in press].
71 Matthew 13:55-56; Mark 6:3.
72 Ugo A. Perego, ‘Current Biology, SMGF, and Lamanites’, (http://www.fairblog.org/2009/02/06/current-biology-smgf-and-lamanites – accessed November 2009).
73 Moroni 10:3-5; Jeffrey R. Holland, ‘Safety for the Soul’, Ensign (November 2009), 88–90 (available at http://lds.org/conference/talk/display/0,5232,23-1-1117-28,00.html – accessed November 2009).